Quality Inspector I at Tegra Medical Holdings LLC
Dartmouth, Massachusetts, United States -
Full Time


Start Date

Immediate

Expiry Date

05 Aug, 26

Salary

23.49

Posted On

07 May, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Visual Inspection, Microscope Operation, ISO 13485, Quality Control, MRP Systems, Technical Writing, Medical Device Manufacturing, Detail Oriented

Industry

Medical Equipment Manufacturing

Description
Job Summary The purpose of the Inspector–I role is to perform visual inspections in order to identify conforming and nonconforming product within the Tegra Medical location.  Role and Responsibilities * Responsible for QC Visual Inspections of finished products required in accordance with ISO 13485. * Accurately perform visual inspection determine acceptability of product from visual defects and other overall cosmetic requirements. * Follow specific internal and customer specifications to determine product conformance. * Act as a trainer for other Inspector–I employees. * Complete inspection reports and product traveler as required. * Keep track of quantities and scrap codes and enter data into MRP system as applicable. * Provide feedback to supervisors and engineering on visual defects found. * Support visual inspection of validation activities as requested. Qualifications * Experience using a microscope is required. * Communication skills verbal and written is required. * Experience in medical device manufacturing is preferred. * Must be able to work with minimal supervision and follow written instruction and schedules. * Must be detail oriented, focused and organized. * Must maintain work areas in a safe and orderly condition at all times. * Must comply with all applicable safety procedures. * Must be able to use microscope for extended periods of time. Education Requirements High School Diploma or equivalent is required. 1st shift 7am to 3:30pm
Responsibilities
Perform visual inspections of finished medical products to ensure conformance with ISO 13485 and customer specifications. Document inspection results in reports and MRP systems while providing feedback on defects to engineering and supervisors.
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